Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909724
rs121909724
MPV17
T 0.700 GeneticVariation CLINVAR Hepatocerebral form of mitochondrial DNA depletion syndrome: novel MPV17 mutations. 18695062

2008
dbSNP: rs121909724
rs121909724
MPV17
T 0.700 CausalMutation CLINVAR